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T10525SCD1 inhibitor-4
SCD1 inhibitor-4 is stearoylCoA desaturase-1 (SCD1) inhibitor. SCD1 inhibitor-4 can be used for the research of diabetes.
价 格:¥电议型 号:T10525产 地:中国大陆
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T0525FlopropionePhloropropiophenone;夫洛丙酮
Flopropione, a spasmolytic or antispasmodic agent, is used as a 5-HT1A receptor antagonist.
价 格:¥电议型 号:T0525产 地:中国大陆
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T11472GSK 525768AGSK 525768A
GSK 525768A has no activity towards BET. GSK 525768A is the inactive enantiomer of GSK525762A.
价 格:¥电议型 号:T11472产 地:美洲
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T11472LMolibresib besylateMolibresib besylate,GSK 525762C,I-BET 762 besylate
Molibresib besylate is an inhibitor of BET bromodomain (IC50: 32.5-42.5 nM).
价 格:¥电议型 号:T11472L产 地:美洲
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T11525GW311616GW311616
GW-311616 is a orally bioavailable,potent , long duration and selective human neutrophil elastase (HNE) inhibitor with IC50 value of 22 nM and Ki value of 0.31 nM.
价 格:¥电议型 号:T11525产 地:美洲
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T11525LGW311616 hydrochlorideGW311616 hydrochloride,GW311616A,
GW-311616 is a potent, long duration,orally bioavailable and selective human neutrophil elastase (HNE) inhibitor with IC50 value of 22 nM and Ki value of 0.31 nM.
价 格:¥电议型 号:T11525L产 地:美洲
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T1156Palonosetron hydrochloridePalonosetron hydrochloride,Palonosetron HCl,RS 25259
Palonosetron is a 5-HT3 antagonist used in the prevention and treatment of chemotherapy-induced nausea and vomiting.
价 格:¥电议型 号:T1156产 地:美洲
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T11847Liarozole dihydrochlorideLiarozole dihydrochloride,R75251 dihydrochloride,
Liarozole dihydrochloride is a cytochrome P450 (CYP450) dependent inhibitor, orally active, it also a potent inhibitor of estrogen (via inhibition of aromatase) and testicular androgen synthesis (inhibition of 17 ,20-lyase).Liarozole dihydrochloride is an
价 格:¥电议型 号:T11847产 地:美洲
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T12525Pozanicline dihydrochloridePozanicline dihydrochloride,ABT-089 dihydrochloride,
Pozanicline dihydrochloride is an orally bioavailable agonist of nicotinic acetylcholine receptor (nAChR) (Ki of 16.7 nM)
价 格:¥电议型 号:T12525产 地:美洲
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T12680(±)-Darifenacin(±)-Darifenacin,(±)-UK-88525,
(±)-Darifenacin is the racemate of Darifenacin. Darifenacin is a selective antagonist of M3 muscarinic receptor.
价 格:¥电议型 号:T12680产 地:美洲
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T13086I-BET762 carboxylic acidI-BET762 carboxylic acid,Molibresib carboxylic acid,GSK525762A carboxylic ac
I-BET762 carboxylic acid is an inhibitor of BRD4(pIC50 of 5.1).
价 格:¥电议型 号:T13086产 地:美洲
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T13525Abiraterone metabolite 1Abiraterone metabolite 1,3β-OH-5α-Abi,
Abiraterone metabolite 1 is a 5β-reduced metabolite of abiraterone. Abiraterone inhibits CYP17A1, blocks androgen synthesis, and prolongs survival in prostate cancer.
价 格:¥电议型 号:T13525产 地:美洲
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T14525BegacestatBegacestat,GSI-953,
Begacestat (GSI-953) is an amyloid precursor protein gamma-secretase (IC50Aβ40=15 nM) inhibitor. Which is used for treatment of Alzheimer´s disease.
价 格:¥电议型 号:T14525产 地:美洲
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T1525RitonavirRitonavir,RTV,ABT 538
Ritonavir is a peptidomimetic agent that inhibits both HIV-1 and HIV-2 proteases. Ritonavir is highly inhibited by serum proteins but boosts the effect of other HIV proteases by blocking their degradation by cytochrome P450.
价 格:¥电议型 号:T1525产 地:美洲
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T15250ETC-206ETC-206
ETC-206 is a selective inhibitor of MNK1 and MNK2 ( IC50s: 64 nM and 86 nM, respectively).
价 格:¥电议型 号:T15250产 地:美洲
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T15255EtilevodopaEtilevodopa,L-DOPA ethyl ester,Levodopa ethyl ester
Etilevodopa is an ethyl-ester prodrug of Levodopa which is used for the treatment of Parkinson disease (PD). It also is rapidly hydrolyzed to Levodopa and ethanol by nonspecific esterases in the gastrointestinal tract. Levodopa is the direct precursor of
价 格:¥电议型 号:T15255产 地:美洲
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T15256Etofylline clofibrateEtofylline clofibrate
Etofylline clofibrate has a hypolipidemic and antithrombotic effect and it also has an agonistic interaction with intimal PGI2.
价 格:¥电议型 号:T15256产 地:美洲
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T15257EtripamilEtripamil,MSP-2017,(-)-MSP-2017
Etripamil displays atrioventricular nodal conduction and prolongs atrioventricular nodal refractory periods by inhibiting calcium ion influx through the calcium slow channels in the atrioventricular node cells. Etripamil is an antagonist of short-acting
价 格:¥电议型 号:T15257产 地:美洲
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T15259EvatanepagEvatanepag,CP-533536 free acid,
Evatanepag is an agonist of EP2 receptor-selective prostaglandin E2 (PGE2). Which induces local bone formation (EC50: 0.3 nM).
价 格:¥电议型 号:T15259产 地:美洲
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T1763SB525334SB525334
SB-525334 is a potent and selective inhibitor of the TGF-β1R and ALK5 (IC50: 14.3 nM).
价 格:¥电议型 号:T1763产 地:美洲